d1c4e8c31212f80abd3c5a25ddff9632

14. KAPA STRANDED RNA-SEQ KIT

ROCHE SEQUENCING SOLUTIONS, INC·I·Colombia INVIMA·Expires February 09, 2033
Device classification
Risk class / Clase de Riesgo
I
Product type (Spanish)
REACTIVOS IN VITRO
Product type (English)
REACTIVOS IN VITRO
Registration information
Analysis ID
d1c4e8c31212f80abd3c5a25ddff9632
Expire date
February 09, 2033
Authorized company / Fabricante
Name (English)
ROCHE SEQUENCING SOLUTIONS, INC
Product use / Uso del Producto
Spanish

LOS REACTIVOS RUO AMPARADOS EN ES ESTE REGISTRO SANITARIO SON REACTIVOS PARA LA PREPARACION DE MUESTRAS, AMPLIFICACION_x000D_ DETECCIÒN Y/O CUANTIFICACIÓN EN MUESTRAS BIOLOGICAS DE ORIGEN HUMANO, DE LOS ACIDOS NUCLÉICOS DNA/RNA. SU PLATAFORMA_x000D_ TECNOLÓGICA ES POR TECNICAS DE BIOLOGIA MOLECULAR POR AMPLIFICACIÓN EN CADENA DE POLIMERASA PCR.

English

THE RUO REAGENTS COVERED IN THIS SANITARY REGISTRY ARE REAGENTS FOR THE PREPARATION OF SAMPLES, AMPLIFICACION_x000D_ DETECTION AND / OR QUANTIFICATION IN BIOLOGICAL SAMPLES OF HUMAN ORIGIN, OF NUCLEIC ACIDS DNA / RNA. YOUR PLATAFORMA_x000D_ TECHNOLOGICAL IS BY MOLECULAR BIOLOGY TECHNIQUES BY PCR POLYMERASE CHAIN AMPLIFICATION.

About this record

Access comprehensive regulatory information for 14. KAPA STRANDED RNA-SEQ KIT (14. KAPA STRANDED RNA-SEQ KIT) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID d1c4e8c31212f80abd3c5a25ddff9632 and manufactured by ROCHE SEQUENCING SOLUTIONS, INC. The device was registered on February 09, 2033.

This page provides complete registration details including product type (REACTIVOS IN VITRO), authorised information, and regulatory compliance data from the official Colombia INVIMA medical device database. Pure Global AI offers free access to Colombia's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate INVIMA regulations efficiently.